A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110513



Internal ID21293779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:87326447..87331309hg38UCSC Ensembl
Innerchr1:87792130..87796992hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg384863
hg194863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv47n145
Supporting Variantsnssv14090940
Samplessample273
Known GenesLMO4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110513
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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